MODIFICATION
A -- Defense Advanced Research Projects Agency (DARPA), Advanced Technology Office (ATO): Advanced Technologies
- Notice Date
- 2/23/2005
- Notice Type
- Modification
- NAICS
- 541710
— Research and Development in the Physical, Engineering, and Life Sciences
- Contracting Office
- Other Defense Agencies, Defense Advanced Research Projects Agency, Contracts Management Office, 3701 North Fairfax Drive, Arlington, VA, 22203-1714
- ZIP Code
- 22203-1714
- Solicitation Number
- BAA05-13
- Response Due
- 12/31/2006
- Archive Date
- 1/15/2007
- Point of Contact
- Anthony Cicala, Contracting Officer, Phone (571)218-4639, Fax (703)248-1927,
- E-Mail Address
-
acicala@darpa.mil
- Description
- The purpose of this modification is to modify the Presolicitation Notice and Proposer Information Pamphlet as follows: 1. Presolicitation Notice. Under the Description section, after TECHNICAL TOPIC AREAS, change "Research supporting any of MTO's broad mission" to "Research supporting any of ATO's broad mission." 2. Proposer Information Pamphlet. Add Paragraph 3.7, Human Use as follows: Proposals selected for funding are required to comply with provisions of the Common Rule (32 CFR 219) on the protection of human subjects in research (http://www.dtic.mil/biosys/downloads/32cfr219.pdf) and the Department of Defense Directive 3216.2 (http://www.dtic.mil/whs/directives/corres/html2/d32162x.htm). All proposals that involve the use of human subjects are required to include documentation of their ability to follow Federal guidelines for the protection of human subjects. This includes, but is not limited to, protocol approval mechanisms, approved Institutional Review Boards, and Federal Wide Assurances. These requirements are based on expected human use issues sometime during the entire length of the proposed effort. For proposals involving "greater than minimal risk" to human subjects within the first year of the project, performers must provide evidence of protocol submission to a federally approved IRB at the time of final proposal submission to DARPA. For proposals that are forecasted to involve "greater than minimal risk" after the first year, a discussion on how and when the proposer will comply with submission to a federally approved IRB needs to be provided in the submission. More information on applicable federal regulations can be found at the Department of Health and Human Services - Office of Human Research Protections website (http://www.dhhs.gov/ohrp/.)
- Record
- SN00757199-W 20050225/050223213016 (fbodaily.com)
- Source
-
FedBizOpps.gov Link to This Notice
(may not be valid after Archive Date)
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